Friday, January 27, 2023 6:06:42 AM
Your post got me to thinking that the perceived delay in MIA approval is not for the manual process of production of DC Vax. This process has been refined, studied and used for years at multiple sites for the trials and compassionate use. There is something "new" to the production process. The delay is the incorporation of Flashworks into the manufacturing to meet future demand. Reference Linda Powers comments in ASM 2022 on December 31, of different flow rates etc. to produce the same results as manual production in a Flashworks unit.
Remember "Laser Focused"
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